Our Web-doc is available!
We follow the journey of three young people with Duchenne muscular dystrophy (DMD). Each view and share will serve to comfort those who suffer from DMD today and will help to heal future generations... Watch it here.
To learn more about Duchenne muscular dystrophy and rare disease, visit our web site, here:
www.laforcedmd.com
Негізгі бет « Living with DMD » What is life like with a rare disease like Duchenne muscular dystrophy?
Пікірлер: 80